Airway Mucus Restricts <named-content content-type="genus-species">Neisseria meningitidis</named-content> Away from Nasopharyngeal Epithelial Cells and Protects the Mucosa from Inflammation

ABSTRACT Neisseria meningitidis is an inhabitant of the nasopharynx, from which it is transmitted from person to person or disseminates in blood and becomes a harmful pathogen. In this work, we addressed colonization of the nasopharyngeal niche by focusing on the interplay between meningococci and t...

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Autores principales: Mathilde Audry, Catherine Robbe-Masselot, Jean-Philippe Barnier, Benoit Gachet, Bruno Saubaméa, Alain Schmitt, Sophia Schönherr-Hellec, Renaud Léonard, Xavier Nassif, Mathieu Coureuil
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Publicado: American Society for Microbiology 2019
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spelling oai:doaj.org-article:d81ef51b21d74508b970f4b3562368012021-11-15T15:22:24ZAirway Mucus Restricts <named-content content-type="genus-species">Neisseria meningitidis</named-content> Away from Nasopharyngeal Epithelial Cells and Protects the Mucosa from Inflammation10.1128/mSphere.00494-192379-5042https://doaj.org/article/d81ef51b21d74508b970f4b3562368012019-12-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00494-19https://doaj.org/toc/2379-5042ABSTRACT Neisseria meningitidis is an inhabitant of the nasopharynx, from which it is transmitted from person to person or disseminates in blood and becomes a harmful pathogen. In this work, we addressed colonization of the nasopharyngeal niche by focusing on the interplay between meningococci and the airway mucus that lines the mucosa of the host. Using Calu-3 cells grown in air interface culture (cells grown with the apical domain facing air), we studied meningococcal colonization of the mucus and the host response. Our results suggested that N. meningitidis behaved like commensal bacteria in mucus, without interacting with human cells or actively transmigrating through the cell layer. As a result, type IV pili do not play a role in this model, and meningococci did not trigger a strong innate immune response from the Calu-3 cells. Finally, we have shown that this model is suitable for studying interaction of N. meningitidis with other bacteria living in the nasopharynx and that Streptococcus mitis, but not Moraxella catarrhalis, can promote meningococcal growth in this model. IMPORTANCE N. meningitidis is transmitted from person to person by aerosol droplets produced by breathing, talking, or coughing or by direct contact with a contaminated fluid. The natural reservoir of N. meningitidis is the human nasopharynx mucosa, located at the back of the nose and above the oropharynx. The means by which meningococci cross the nasopharyngeal wall is still under debate, due to the lack of a convenient and relevant model mimicking the nasopharyngeal niche. Here, we took advantage of Calu-3 cells grown in air interface culture to study how meningococci colonize the nasopharyngeal niche. We report that the airway mucus is both a niche for meningococcal growth and a protective barrier against N. meningitidis infection. As such, N. meningitidis behaves like commensal bacteria and is unlikely to induce infection without an external trigger.Mathilde AudryCatherine Robbe-MasselotJean-Philippe BarnierBenoit GachetBruno SaubaméaAlain SchmittSophia Schönherr-HellecRenaud LéonardXavier NassifMathieu CoureuilAmerican Society for Microbiologyarticleairway mucushost-pathogen interactionmeningitisnasopharynxNeisseria meningitidisMicrobiologyQR1-502ENmSphere, Vol 4, Iss 6 (2019)
institution DOAJ
collection DOAJ
language EN
topic airway mucus
host-pathogen interaction
meningitis
nasopharynx
Neisseria meningitidis
Microbiology
QR1-502
spellingShingle airway mucus
host-pathogen interaction
meningitis
nasopharynx
Neisseria meningitidis
Microbiology
QR1-502
Mathilde Audry
Catherine Robbe-Masselot
Jean-Philippe Barnier
Benoit Gachet
Bruno Saubaméa
Alain Schmitt
Sophia Schönherr-Hellec
Renaud Léonard
Xavier Nassif
Mathieu Coureuil
Airway Mucus Restricts <named-content content-type="genus-species">Neisseria meningitidis</named-content> Away from Nasopharyngeal Epithelial Cells and Protects the Mucosa from Inflammation
description ABSTRACT Neisseria meningitidis is an inhabitant of the nasopharynx, from which it is transmitted from person to person or disseminates in blood and becomes a harmful pathogen. In this work, we addressed colonization of the nasopharyngeal niche by focusing on the interplay between meningococci and the airway mucus that lines the mucosa of the host. Using Calu-3 cells grown in air interface culture (cells grown with the apical domain facing air), we studied meningococcal colonization of the mucus and the host response. Our results suggested that N. meningitidis behaved like commensal bacteria in mucus, without interacting with human cells or actively transmigrating through the cell layer. As a result, type IV pili do not play a role in this model, and meningococci did not trigger a strong innate immune response from the Calu-3 cells. Finally, we have shown that this model is suitable for studying interaction of N. meningitidis with other bacteria living in the nasopharynx and that Streptococcus mitis, but not Moraxella catarrhalis, can promote meningococcal growth in this model. IMPORTANCE N. meningitidis is transmitted from person to person by aerosol droplets produced by breathing, talking, or coughing or by direct contact with a contaminated fluid. The natural reservoir of N. meningitidis is the human nasopharynx mucosa, located at the back of the nose and above the oropharynx. The means by which meningococci cross the nasopharyngeal wall is still under debate, due to the lack of a convenient and relevant model mimicking the nasopharyngeal niche. Here, we took advantage of Calu-3 cells grown in air interface culture to study how meningococci colonize the nasopharyngeal niche. We report that the airway mucus is both a niche for meningococcal growth and a protective barrier against N. meningitidis infection. As such, N. meningitidis behaves like commensal bacteria and is unlikely to induce infection without an external trigger.
format article
author Mathilde Audry
Catherine Robbe-Masselot
Jean-Philippe Barnier
Benoit Gachet
Bruno Saubaméa
Alain Schmitt
Sophia Schönherr-Hellec
Renaud Léonard
Xavier Nassif
Mathieu Coureuil
author_facet Mathilde Audry
Catherine Robbe-Masselot
Jean-Philippe Barnier
Benoit Gachet
Bruno Saubaméa
Alain Schmitt
Sophia Schönherr-Hellec
Renaud Léonard
Xavier Nassif
Mathieu Coureuil
author_sort Mathilde Audry
title Airway Mucus Restricts <named-content content-type="genus-species">Neisseria meningitidis</named-content> Away from Nasopharyngeal Epithelial Cells and Protects the Mucosa from Inflammation
title_short Airway Mucus Restricts <named-content content-type="genus-species">Neisseria meningitidis</named-content> Away from Nasopharyngeal Epithelial Cells and Protects the Mucosa from Inflammation
title_full Airway Mucus Restricts <named-content content-type="genus-species">Neisseria meningitidis</named-content> Away from Nasopharyngeal Epithelial Cells and Protects the Mucosa from Inflammation
title_fullStr Airway Mucus Restricts <named-content content-type="genus-species">Neisseria meningitidis</named-content> Away from Nasopharyngeal Epithelial Cells and Protects the Mucosa from Inflammation
title_full_unstemmed Airway Mucus Restricts <named-content content-type="genus-species">Neisseria meningitidis</named-content> Away from Nasopharyngeal Epithelial Cells and Protects the Mucosa from Inflammation
title_sort airway mucus restricts <named-content content-type="genus-species">neisseria meningitidis</named-content> away from nasopharyngeal epithelial cells and protects the mucosa from inflammation
publisher American Society for Microbiology
publishDate 2019
url https://doaj.org/article/d81ef51b21d74508b970f4b356236801
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